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Trial Review
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Trial registered on ANZCTR
Registration number
ACTRN12621001319864
Ethics application status
Approved
Date submitted
1/07/2021
Date registered
28/09/2021
Date last updated
30/08/2022
Date data sharing statement initially provided
28/09/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
Real world management and outcome of melanoma patients in Australasia using the MASTER registry.
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Scientific title
Real world management and outcome of melanoma patients in Australasia using the MASTER registry (MASTER: MelanomA data to capture Standard of care Treatment and outcomEs and to support Research)
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Secondary ID [1]
305315
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Melanoma
322625
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Condition category
Condition code
Cancer
320246
320246
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0
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Malignant melanoma
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Intervention/exposure
Study type
Observational
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Patient registry
True
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Target follow-up duration
5
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Target follow-up type
Years
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Description of intervention(s) / exposure
The follow up period is a minimum of 12 months (and up to 5 years) with extension dependent on funding of registry. Follow up frequency is approximately every 3-6 months. No additional tests are required. The project will capture data from the medical record of patients with histological or cytological confirmed stage III or IV melanoma from January 2020 onwards, from HREC approved sites within Australasia. Information regarding the multi-disciplinary management of melanoma will be collected, including surgery, radiotherapy, systemic therapy and palliative care in the routine clinical practice setting.
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Intervention code [1]
321030
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Exploring the characteristics of both disease and patients by assessing medical records every 3-6 months.
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Assessment method [1]
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Timepoint [1]
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Every 3-6 months for a minimum of 12 months and a maximum of 5 years.
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Primary outcome [2]
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Treatment patterns (regimen/agent, line of therapy) by assessing medical records every 3-6 months .
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Assessment method [2]
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Timepoint [2]
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Every 3-6 months for a minimum of 12 months and a maximum of 5 years.
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Primary outcome [3]
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Management of patients (including surgery) by assessing medical records every 3-6 months .
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Assessment method [3]
328961
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Timepoint [3]
328961
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Every 3-6 months for a minimum of 12 months and a maximum of 5 years.
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Secondary outcome [1]
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Nil
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Assessment method [1]
400949
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Timepoint [1]
400949
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Nil
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Eligibility
Key inclusion criteria
1. Patient with stage III or IV cutaneous or unknown primary melanoma
2. Aged 18 years or above at diagnosis
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
None
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Both
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Statistical methods / analysis
Descriptive statistics will be the primary analysis used to present data from this study,
covering epidemiological measures of interest such as population composition, incidence rates, observed event rates and outcome measures including survival time and hazard ratios/confidence intervals where appropriate for intergroup comparisons.
As this is a descriptive study and no hypothesis will be tested, no formal sample size and power calculations were performed.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
4/10/2021
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Actual
8/04/2022
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Date of last participant enrolment
Anticipated
30/12/2022
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Actual
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Date of last data collection
Anticipated
29/12/2023
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Actual
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Sample size
Target
200
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Accrual to date
42
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
19866
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Box Hill Hospital - Box Hill
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Recruitment hospital [2]
19867
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Maroondah Hospital - Ringwood East
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Recruitment hospital [3]
19868
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Yarra Ranges Health - Lilydale
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Recruitment hospital [4]
19869
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Epworth Eastern Hospital - Box Hill
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Recruitment hospital [5]
19870
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The Alfred - Melbourne
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Recruitment hospital [6]
19871
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Royal Melbourne Hospital - Royal Park campus - Parkville
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Recruitment hospital [7]
19872
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Peter MacCallum Cancer Centre - Melbourne
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Recruitment hospital [8]
19873
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Austin Health - Austin Hospital - Heidelberg
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Recruitment hospital [9]
19874
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Cabrini Hospital - Malvern - Malvern
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Recruitment hospital [10]
19875
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Barwon Health - Geelong Hospital campus - Geelong
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Recruitment postcode(s) [1]
34569
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3128 - Box Hill
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Recruitment postcode(s) [2]
34570
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3135 - Ringwood East
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Recruitment postcode(s) [3]
34571
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3140 - Lilydale
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Recruitment postcode(s) [4]
34572
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3004 - Melbourne
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Recruitment postcode(s) [5]
34573
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3052 - Parkville
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Recruitment postcode(s) [6]
34574
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3084 - Heidelberg
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Recruitment postcode(s) [7]
34575
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3144 - Malvern
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Recruitment postcode(s) [8]
34576
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3220 - Geelong
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Funding & Sponsors
Funding source category [1]
309036
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Commercial sector/Industry
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Name [1]
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Merck Sharp & Dohme (Australia) Pty Ltd
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Address [1]
309036
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MSD Level 1, 26 Talavera Road
Macquarie Park, NSW 2113
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Country [1]
309036
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Australia
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Primary sponsor type
Other Collaborative groups
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Name
The Walter and Eliza Hall Institute of Medical Research
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Address
1G Royal Parade, Parkville VIC 3052
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Country
Australia
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Secondary sponsor category [1]
309972
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Commercial sector/Industry
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Name [1]
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Merck Sharp & Dohme (Australia) Pty Ltd
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Address [1]
309972
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MSD Level 1, 26 Talavera Road
Macquarie Park NSW 2113
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Country [1]
309972
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
308914
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Melbourne Health HREC
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Ethics committee address [1]
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Office for Research Level 2, South West 300 Grattan Street Parkville VIC 3050
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
308914
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25/11/2020
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Approval date [1]
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02/06/2021
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Ethics approval number [1]
308914
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Summary
Brief summary
The aim of this study (registry) is to document diagnosis, treatment and outcomes for patients with advanced melanoma over time, in order to better understand survival and treatment efficacy in these patients. Who is it for? You may be eligible for this study if you are aged 18 years or older, and have been diagnosed with stage III or IV cutaneous or unknown primary melanoma. Study details Information regarding the multi-disciplinary management of melanoma, including surgery, radiotherapy, systemic therapy, and palliative care in the routine clinical practice setting is obtained via medical records. Information regarding the clinical outcomes of treatment, including time to disease progression and overall survival, will also be collected. Participants will be followed up for a minimum of 12 months and a maximum of 5 years, if funding for this extension can be secured. No additional tests or time commitment by participants is required. It is hoped that this study will allow a comprehensive analysis of melanoma diagnosis, treatment and outcomes, supporting much needed basic, translational and clinical research of this disease. This may help to provide insight into optimal management of advanced melanoma in light of new and emerging treatments.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Peter Gibbs
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Address
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Gibbs Laboratory
Personalised Oncology Division
The Walter and Eliza Hall Institute of Medical Research (WEHI)
1G Royal Parade
Parkville VIC 3052
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Country
112326
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Australia
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Phone
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+61 3 9345 2897
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Fax
112326
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Email
112326
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[email protected]
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Contact person for public queries
Name
112327
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Miles Andrews
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Address
112327
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Gibbs Laboratory
Personalised Oncology Division
The Walter and Eliza Hall Institute of Medical Research (WEHI)
1G Royal Parade
Parkville VIC 3052
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Country
112327
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Australia
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Phone
112327
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+61 3 9345 2880
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Fax
112327
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Email
112327
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[email protected]
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Contact person for scientific queries
Name
112328
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Miles Andrews
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Address
112328
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Gibbs Laboratory
Personalised Oncology Division
The Walter and Eliza Hall Institute of Medical Research (WEHI)
1G Royal Parade
Parkville VIC 3052
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Country
112328
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Australia
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Phone
112328
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+61 3 9345 2880
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Fax
112328
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Email
112328
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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